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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
February 21, 2012
Polymerase gamma deficiency (POLG): clinical course in a child with a two stage evolution from infantile myocerebrohepatopathy spectrum to an Alpers syndrome and neuropathological findings of Leigh's encephalopathy
Emmanuel Scalais, Baudouin Francois, Patrick Schlesser, et al.
Mitochondrion
|
April 25, 2009
Pathogenic mutations in the 5' untranslated region of BCS1L mRNA in mitochondrial complex III deficiency
M Carmen Gil-Borlado, Maritza González-Hoyuela, Alberto Blázquez, et al.
Brain : a Journal of Neurology
|
October 7, 2023
Sustained OMA1-mediated integrated stress response is beneficial for spastic ataxia type 5
Camilla Aurora Franchino, Martina Brughera, Valentina Baderna, et al.
Pediatric Research
|
December 6, 2005
Diagnostic value of immunostaining in cultured skin fibroblasts from patients with oxidative phosphorylation defects
Boel de Paepe, Joél Smet, Jules G Leroy, et al.
Stem Cell Reports
|
June 19, 2018
Random Mutagenesis, Clonal Events, and Embryonic or Somatic Origin Determine the mtDNA Variant Type and Load in Human Pluripotent Stem Cells
Filippo Zambelli, Joke Mertens, Dominika Dziedzicka, et al.
The Journal of Biological Chemistry
|
November 26, 2009
Defining the pathogenesis of the human Atp12p W94R mutation using a Saccharomyces cerevisiae yeast model
Ann Meulemans, Sara Seneca, Thomas Pribyl, et al.
Journal of Inherited Metabolic Disease
|
May 15, 2015
Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy
François-Guillaume Debray, Claudia Stümpfig, Arnaud V Vanlander, et al.
Mitochondrion
|
February 9, 2016
Megaconial muscular dystrophy caused by mitochondrial membrane homeostasis defect, new insights from skeletal and heart muscle analyses
Arnaud V Vanlander, Laura Muiño Mosquera, Joseph Panzer, et al.
Nature Communications
|
December 3, 2025
Vacuolar-type H<sup>+</sup>-ATPase-mediated extra-organellar buffering resolves mitochondrial dysfunction
Geoffray Monteuuis, Ryan Awadhpersad, Daan van der Kolk, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
April 1, 2006
Linezolid-induced inhibition of mitochondrial protein synthesis
An S De Vriese, Rudy Van Coster, Joel Smet, et al.
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Search research articles
Search
Showing results (61-70 of 88) with videos related to
Sort By:
Page
of 9
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
February 21, 2012
Polymerase gamma deficiency (POLG): clinical course in a child with a two stage evolution from infantile myocerebrohepatopathy spectrum to an Alpers syndrome and neuropathological findings of Leigh's encephalopathy
Emmanuel Scalais, Baudouin Francois, Patrick Schlesser, et al.
Mitochondrion
|
April 25, 2009
Pathogenic mutations in the 5' untranslated region of BCS1L mRNA in mitochondrial complex III deficiency
M Carmen Gil-Borlado, Maritza González-Hoyuela, Alberto Blázquez, et al.
Brain : a Journal of Neurology
|
October 7, 2023
Sustained OMA1-mediated integrated stress response is beneficial for spastic ataxia type 5
Camilla Aurora Franchino, Martina Brughera, Valentina Baderna, et al.
Pediatric Research
|
December 6, 2005
Diagnostic value of immunostaining in cultured skin fibroblasts from patients with oxidative phosphorylation defects
Boel de Paepe, Joél Smet, Jules G Leroy, et al.
Stem Cell Reports
|
June 19, 2018
Random Mutagenesis, Clonal Events, and Embryonic or Somatic Origin Determine the mtDNA Variant Type and Load in Human Pluripotent Stem Cells
Filippo Zambelli, Joke Mertens, Dominika Dziedzicka, et al.
The Journal of Biological Chemistry
|
November 26, 2009
Defining the pathogenesis of the human Atp12p W94R mutation using a Saccharomyces cerevisiae yeast model
Ann Meulemans, Sara Seneca, Thomas Pribyl, et al.
Journal of Inherited Metabolic Disease
|
May 15, 2015
Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy
François-Guillaume Debray, Claudia Stümpfig, Arnaud V Vanlander, et al.
Mitochondrion
|
February 9, 2016
Megaconial muscular dystrophy caused by mitochondrial membrane homeostasis defect, new insights from skeletal and heart muscle analyses
Arnaud V Vanlander, Laura Muiño Mosquera, Joseph Panzer, et al.
Nature Communications
|
December 3, 2025
Vacuolar-type H<sup>+</sup>-ATPase-mediated extra-organellar buffering resolves mitochondrial dysfunction
Geoffray Monteuuis, Ryan Awadhpersad, Daan van der Kolk, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
April 1, 2006
Linezolid-induced inhibition of mitochondrial protein synthesis
An S De Vriese, Rudy Van Coster, Joel Smet, et al.
Page
of 9